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diagnosis differential 21hydroxylasedeficiency 21ohd agammaglobulinemia brudzinskis clinical dyspnea endocrinology floppy hypotonic iem immunology inbornerrors incomplete infant kawasaki meningitis metabolicemergency metabolism
A schema of the pathophysiology of the inborn errors of metabolism, excluding complex storage diseases. Helps
complex storage diseases ... MetabolicEmergency #Genetics ... #Pathophysiology ... #Diagnosis #Algorithm ... #Neonatology #Peds
Pediatric Dyspnea - Differential Diagnosis Algorithm Stridor: • Croup • Foreign Body • Tracheitis • Epiglottitis •
Pediatric Dyspnea ... Foreign Body Decreased ... Body • Heart Disease ... #Causes #Peds # ... Pediatrics
Causes of Hypotonic Infant (Floppy Newborn) - Differential Diagnosis Algorithm Central Nervous System - Decreased LOC, Axial
Causes of Hypotonic ... Differential Diagnosis Algorithm ... Nervous System - Decreased ... #Causes #Peds # ... Pediatrics
Brudzinski’s Sign in Meningitis (first described in 19th century by Dr. Josef Brudzinski) Brudzinski's sign is characterized
Passive neck flexion causes ... While the pathophysiology ... despite severe disease ... #PhysicalExam #Pediatrics ... #Peds
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 X-Linked Agammaglobulinemia: Pathogenesis and clinical findings The epidemiology of this disease is 1/340,000 births and roughly double
epidemiology of this disease ... history of the disease ... Genetic Predisposition ... to produce all classes ... Agammaglobulinemia #XLinked #pathophysiology
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
enzyme 21-OHase causes ... Signs/Symptoms/Complications ... #21HydroxylaseDeficiency #21OHD #pathophysiology ... #genetics #endocrinology ... #peds #pediatrics
Evaluation of suspected incomplete Kawasaki Disease 1. AHA consensus recommendations 2. Infants ≤6 months old on day ≥7
lack of tapering, decreased ... clinical and lab signs ... #Diagnosis #Peds ... #Pediatrics #Kawasaki ... #Algorithm
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